Health research involves analyzing millions of patient records with the goal of better understanding human diseases, to determine treatment effectiveness, and to identify health and disease trends. However, HIPAA law requires patients to give approval for their records to be used in this kind of study, and many patients do not understand what is being asked of them when permission is requested. What impacts might this have on the speed of and quality of health research? What recommendations can you make to resolve the impacts you identified?

Health research involves analyzing millions of patient records with the goal of better understanding human diseases, to determine treatment effectiveness, and to identify health and disease trends. However, HIPAA law requires patients to give approval for their records to be used in this kind of study, and many patients do not understand what is being asked of them when permission is requested. What impacts might this have on the speed of and quality of health research? What recommendations can you make to resolve the impacts you identified?

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